Synthesis of oxygenated heterocycles from cyclic allylsiloxanes using ring-closing olefin metathesis
β Scribed by Christophe Meyer; Janine Cossy
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 180 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Cyclic ailylsiloxanes were prepared from allyldimethylsilyl ethers of various aikenols by using a catalytic ring-clusing metathcsis (RCM) reaclion. The transformation of these cyclic ailyls/loxanes into stereuseiectively substituted tetrahydrofurans and tetrahydropyrans was achieved by using a silyl modified Sakurai reaction.
π SIMILAR VOLUMES
prepared in a one-step procedure by ring closing metathesis of dienes 7aΒ±k.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v